Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2294450
rs2294450
Entrez Id: 51764;63922
Gene Symbol: GNG13;CHTF18
GNG13;CHTF18
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2277899
rs2277899
Entrez Id: 63922;113000
Gene Symbol: CHTF18;RPUSD1
CHTF18;RPUSD1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs742320
rs742320
Entrez Id: 63922
Gene Symbol: CHTF18
CHTF18
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016